meddevicedb.com FDA Device Reference

PRORAD X-Ray Flat Panel Detector with DROC

K240771 Class II Traditional
Decision Date
2024-11-12
Sponsor / Applicant
Prognosys Medical Systems Private Limited

Technical Specification

510(k) Submission ID K240771
Product Code MQB
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1680
Decision Date 2024-11-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PRORAD X-Ray Flat Panel Detector with DROC received FDA 510(k) clearance under submission number K240771, sponsored by Prognosys Medical Systems Private Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2024-11-12.

Classification & Regulation

This clearance is catalogued under FDA product code MQB and 21 CFR 892.1680, within the Radiology review panel as a Class II device.